rs767830104, CXCR4

N. diseases: 13
Source: BEFREE ×
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1022 0.752 0.280 2 136115399 missense variant C/G;T snv 4.0E-06; 8.0E-06 0.050 1.000 5 2001 2012
Coronary Arteriosclerosis
CUI: C0010054
Disease: Coronary Arteriosclerosis
440 0.752 0.280 2 136115399 missense variant C/G;T snv 4.0E-06; 8.0E-06 0.020 1.000 2 2008 2012
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
769 0.752 0.280 2 136115399 missense variant C/G;T snv 4.0E-06; 8.0E-06 0.020 1.000 2 2008 2012
Acquired Immunodeficiency Syndrome
CUI: C0001175
Disease: Acquired Immunodeficiency Syndrome
14 0.752 0.280 2 136115399 missense variant C/G;T snv 4.0E-06; 8.0E-06 0.010 1.000 1 2005 2005
Acute myocardial infarction
CUI: C0155626
Disease: Acute myocardial infarction
118 0.752 0.280 2 136115399 missense variant C/G;T snv 4.0E-06; 8.0E-06 0.010 1.000 1 2012 2012
Age related macular degeneration
CUI: C0242383
Disease: Age related macular degeneration
390 0.752 0.280 2 136115399 missense variant C/G;T snv 4.0E-06; 8.0E-06 0.010 1.000 1 2004 2004
Anthracosis
CUI: C0003165
Disease: Anthracosis
37 0.752 0.280 2 136115399 missense variant C/G;T snv 4.0E-06; 8.0E-06 0.010 1.000 1 2006 2006
Cardiovascular Abnormalities
CUI: C0243050
Disease: Cardiovascular Abnormalities
4 0.752 0.280 2 136115399 missense variant C/G;T snv 4.0E-06; 8.0E-06 0.010 1.000 1 2003 2003
Chronic kidney disease stage 5
CUI: C2316810
Disease: Chronic kidney disease stage 5
188 0.752 0.280 2 136115399 missense variant C/G;T snv 4.0E-06; 8.0E-06 0.010 1.000 1 2003 2003
Kidney Failure, Chronic
CUI: C0022661
Disease: Kidney Failure, Chronic
191 0.752 0.280 2 136115399 missense variant C/G;T snv 4.0E-06; 8.0E-06 0.010 1.000 1 2003 2003
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
547 0.752 0.280 2 136115399 missense variant C/G;T snv 4.0E-06; 8.0E-06 0.010 1.000 1 2016 2016
Parkinson Disease
CUI: C0030567
Disease: Parkinson Disease
751 0.752 0.280 2 136115399 missense variant C/G;T snv 4.0E-06; 8.0E-06 0.010 1.000 1 2012 2012
Peripheral Arterial Diseases
CUI: C1704436
Disease: Peripheral Arterial Diseases
54 0.752 0.280 2 136115399 missense variant C/G;T snv 4.0E-06; 8.0E-06 0.010 1.000 1 2003 2003